Related Experiment Video
Updated: Mar 9, 2026

An Orthotopic Bladder Cancer Model for Gene Delivery Studies
Published on: December 1, 2013
Epigenetic therapy in urologic cancers: an update on clinical trials
Inês Faleiro1,2,3, Ricardo Leão4,5, Alexandra Binnie1,2,3
1Regenerative Medicine Program, Department of Biomedical Sciences and Medicine, University of Algarve, Faro, Portugal.
Abstract:
Epigenetic dysregulation is one of many factors that contribute to cancer development and progression. Numerous epigenetic alterations have been identified in urologic cancers including histone modifications, DNA methylation changes, and microRNA expression. Since these changes are reversible, efforts are being made to develop epigenetic drugs that restore the normal epigenetic patterns of cells, and many clinical trials are already underway to test their clinical potential. In this review we analyze multiple clinical trials (n=51) that test the efficacy of these drugs in patients with urologic cancers. The most frequently used epigenetic drugs were histone deacetylase inhibitors followed by antisense oligonucleotides, DNA methyltransferase inhibitors and histone demethylase inhibitors, the last of which are only being tested in prostate cancer. In more than 50% of the clinical trials considered, epigenetic drugs were used as part of combination therapy, which achieved the best results. The epigenetic regulation of some cancers is still matter of research but will undoubtedly open a window to new therapeutic approaches in the era of personalized medicine. The future of therapy for urological malignancies is likely to include multidrug regimens in which epigenetic modifying drugs will play an important role.
Insights
Epigenetic drugs show promise for urologic cancers by reversing abnormal epigenetic patterns. Combination therapies involving these drugs yielded the best outcomes in clinical trials.
Area of Science:
- Oncology
- Epigenetics
- Urologic Cancers
Background:
- Epigenetic dysregulation, including histone modifications, DNA methylation, and microRNA changes, contributes to urologic cancer development.
- These epigenetic alterations are reversible, presenting opportunities for therapeutic intervention.
Purpose of the Study:
- To review clinical trials evaluating epigenetic drugs in patients with urologic cancers.
- To analyze the efficacy and common drug classes used in these trials.
Main Methods:
- Systematic review of 51 clinical trials involving epigenetic drugs for urologic cancers.
- Analysis of drug types, combination therapies, and outcomes.
Main Results:
- Histone deacetylase inhibitors were the most common epigenetic drugs used, followed by antisense oligonucleotides and DNA methyltransferase inhibitors.
- Histone demethylase inhibitors were exclusively tested in prostate cancer.
- Combination therapy, involving epigenetic drugs alongside other treatments, was employed in over 50% of trials and demonstrated superior results.
Conclusions:
- Epigenetic drugs, particularly in combination regimens, represent a significant therapeutic avenue for urological malignancies.
- Further research into epigenetic regulation will drive personalized medicine approaches for these cancers.
More Related Videos
07:25A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
10:27Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
Treatment Resistant Cancers
Gene Therapy
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...